ZMP
ift81
Ensembl ID:
ZFIN ID:
Description:
intraflagellar transport protein 81 homolog [Source:RefSeq peptide;Acc:NP_001002313]
Human Orthologue:
IFT81
Human Description:
intraflagellar transport 81 homolog (Chlamydomonas) [Source:HGNC Symbol;Acc:14313]
Mouse Orthologue:
Ift81
Mouse Description:
intraflagellar transport 81 homolog (Chlamydomonas) Gene [Source:MGI Symbol;Acc:MGI:1098597]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7332 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| hu7911 | Nonsense | Available for shipment | Available now |
| sa41136 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31633 | Essential Splice Site | Available for shipment | Available now |
| sa38673 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14146 | Nonsense | Available for shipment | Available now |
| sa34331 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7332
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Nonsense | 11 | 675 | 1 | 18 |
| ENSDART00000004288 | Nonsense | 11 | 675 | 1 | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12159905)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11604668 |
| GRCz11 | 8 | 11642373 |
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays)
KASP Sequence:
CACTAACGNNNNNNTAATTCTTCAARATGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGAC
Long Flanking Sequence:
ATCATTTTATCCAGTTAATTATATAGTGTATAGATTCCCTATATCATAATATATTATTAATTTTTTTAAACATCTTACGTTACTGATTATTGTTTAGTTTCAAAAAGAGTTAAAAGTCTTTTATGGGGACTTTTACTTTAAAAAGTAGGAAATCTCTTCACATTGTCCAACTTCCTGCTAGCAACCGGGCCTTGTGTGACAACGGTTTCTAGGCAGGATTTGTTGACGTGAGAGGGAACGTTATACGACGTTATTATACAAAAATTTATTATCGTTTTCATTCATCTAAAATCAAATATTAAACGACATTCTGTGCTTGCGCTACAAAAGCTATAATACGGTAAATAATTCGGCTGTTAGCTGCTAACGTGAGTTGGAAAAGTTATTTTGAACACATCGCAAGCTAACGGAAGTTAACGTTGTGAGAATATTTTTGTTAGCGGTAAAAGCCACTAACGTAATTCTTCAAGATGAGCGAACAGCTTAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGACTCTCTGGAGCCAATGCAGCTTCTGCAGACTTTAAGTGATGTTCTGGCTGAAATTGATCCAAAGGTAAGTTGAAGATCAAATTTAATATGACTAATAAAACCACAACCTATAGCAATACATATCTATAATAGTACATAGTATCAAAACGGTAAATAAAAGTAGGGCTTCACGTTATTTTATTTTTCTGCAGTTTCAGAAGATGGTTTAAATAGCTTTATTTGATTGTTTTTTTCTATGCAGTCTAACAGTATTCGGGTAACAGAAATTAAATAATCACAATGTAAAAAAATGCATTTCTTAACTTGCTTTGTTTTGTCTCGTTTTTAGTTACAAATATACAAACAATTTCTAAGACTAAGTAAAGATGCTGTTTAGTTTTAATCGTCCAAATAAAGTAAAAAATTAAAAAAAATTGTTTTAAGAGTTTTATCTTTTGTTTTAAGTGGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7911
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Nonsense | 11 | 675 | 1 | 18 |
| ENSDART00000004288 | Nonsense | 11 | 675 | 1 | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12159905)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11604668 |
| GRCz11 | 8 | 11642373 |
KASP Assay ID:
554-2408.1 (used for ordering genotyping assays)
KASP Sequence:
CACTAACGNNNNNNTAAYKYTTYAAGRWGAGCGAACAGCTYAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTASATTCGAC
Long Flanking Sequence:
ATCATTTTATCCAGTTAATTATATAGTGTATAGATTCCCTATATCATAATATATTATTAATTTTTTTAAACATCTTACGTTACTGATTATTGTTTAGTTTCAAAAAGAGTTAAAAGTCTTTTATGGGGACTTTTACTTTAAAAAGTAGGAAATCTCTTCACATTGTCCAACTTCCTGCTAGCAACCGGGCCTTGTGTGACAACGGTTTCTAGGCAGGATTTGTTGACGTGAGAGGGAACGTTATACGACGTTATTATACAAAAATTTATTATCGTTTTCATTCATCTAAAATCAAATATTAAACGACATTCTGTGCTTGCGCTACAAAAGCTATAATACGGTAAATAATTCGGCTGTTAGCTGCTAACGTGAGTTGGAAAAGTTATTTTGAACACATCGCAAGCTAACGGAAGTTAACGTTGTGAGAATATTTTTGTTAGCGGTAAAAGCCACTAACGTAATTCTTCAAGATGAGCGAACAGCTTAAATTTATCGTTGAA[C/T]AGCTGAACAAGGAGCCTTTCAAGAAAAACTTCAATCTCATTACATTCGACTCTCTGGAGCCAATGCAGCTTCTGCAGACTTTAAGTGATGTTCTGGCTGAAATTGATCCAAAGGTAAGTTGAAGATCAAATTTAATATGACTAATAAAACCACAACCTATAGCAATACATATCTATAATAGTACATAGTATCAAAACGGTAAATAAAAGTAGGGCTTCACGTTATTTTATTTTTCTGCAGTTTCAGAAGATGGTTTAAATAGCTTTATTTGATTGTTTTTTTCTATGCAGTCTAACAGTATTCGGGTAACAGAAATTAAATAATCACAATGTAAAAAAATGCATTTCTTAACTTGCTTTGTTTTGTCTCGTTTTTAGTTACAAATATACAAACAATTTCTAAGACTAAGTAAAGATGCTGTTTAGTTTTAATCGTCCAAATAAAGTAAAAAATTAAAAAAAATTGTTTTAAGAGTTTTATCTTTTGTTTTAAGTGGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41136
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Nonsense | 70 | 675 | 2 | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12161709)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11606472 |
| GRCz11 | 8 | 11644177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTG[G/T]GAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTGTAAGACAGA
Long Flanking Sequence:
GCAATATCGATGCTGAAACTATATGTTGTGCAGCCCTAATGTAAAGGATAGTTCACACCATACTGAAAACTTCATTTACATCATTTACTTTATTTGTTCCAAGCTGGTTTGACTTTCTTCTGTTGAACCACTGACTTGCATAGTATTTGTTTATCCCAACTTTAGAAGTCAATAGTCACAATTTTTAAGTTTTCTGCAAAATATCTACTTTAATATTTAACAGAATAAAGAATTACAAAAAGTTTCAAAACCTCTTGAAGATGAGTAAATAGTGAGCAATTTTTCATTTTTGGGTGAACAAGGCCTTTAATATTCTTTCACAGTTTCCTTTGAAACCACATTTTATTTTTAGAGAGTACTGTATAGATCTTTATTTATGTAATGTGTTCACACTGATAGTTTTTGACACTTTTTCTTTTTTCTGAATCTTTTTTCAGCAAGCCATTGATATACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTG[G/T]GAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTGTAAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATTTATTCCAGTGATTTTAAAGATGATTTTTCAACTTCATTACTCCAGTCTTCATGATCCTTCAGAAATCACTCTGATATGAATTATTATTATTATTATTGTTATTATTATTATGAATGCTATATAATAAAAGCAATAATGACTGGAGTAATAATTTCATTTGAAACTACATTTAATAAGAAAGCAGTTATTTAGAATTGTGATAAATATTTTTAAAAAGTTTACATTTAATAAATGCTACTTTGATGAACAGAATGGTTTTTTTTTTAAAACATGGAGGAAAAAAAACAATATATATATATATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTATTTTCTTCGTACTTCACACATCTAATCAGCTTTAAAATGTCGATTGAACAGAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31633
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Essential Splice Site | 83 | 675 | 2 | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12161751)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11606514 |
| GRCz11 | 8 | 11644219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATT
Long Flanking Sequence:
AAAGGATAGTTCACACCATACTGAAAACTTCATTTACATCATTTACTTTATTTGTTCCAAGCTGGTTTGACTTTCTTCTGTTGAACCACTGACTTGCATAGTATTTGTTTATCCCAACTTTAGAAGTCAATAGTCACAATTTTTAAGTTTTCTGCAAAATATCTACTTTAATATTTAACAGAATAAAGAATTACAAAAAGTTTCAAAACCTCTTGAAGATGAGTAAATAGTGAGCAATTTTTCATTTTTGGGTGAACAAGGCCTTTAATATTCTTTCACAGTTTCCTTTGAAACCACATTTTATTTTTAGAGAGTACTGTATAGATCTTTATTTATGTAATGTGTTCACACTGATAGTTTTTGACACTTTTTCTTTTTTCTGAATCTTTTTTCAGCAAGCCATTGATATACGTGAGGAATTGCCTGAGCAGACAGCCAAGAGAATGTTCACTCTTCTGGGAATGCTGAAATACAAACCTTCTGGAGGAATGTCTGAAGTG[T/C]AAGACAGAAAATAACTGTTCAAAAGTAGTTTATAATGTAATTTAATCATTTATTCCAGTGATTTTAAAGATGATTTTTCAACTTCATTACTCCAGTCTTCATGATCCTTCAGAAATCACTCTGATATGAATTATTATTATTATTATTGTTATTATTATTATGAATGCTATATAATAAAAGCAATAATGACTGGAGTAATAATTTCATTTGAAACTACATTTAATAAGAAAGCAGTTATTTAGAATTGTGATAAATATTTTTAAAAAGTTTACATTTAATAAATGCTACTTTGATGAACAGAATGGTTTTTTTTTTAAAACATGGAGGAAAAAAAACAATATATATATATATATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTATTTTCTTCGTACTTCACACATCTAATCAGCTTTAAAATGTCGATTGAACAGAAGCAGTTTTCGTCAGGGTTTGGTGTCGGGCAGTAAGCCTGTGGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38673
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Nonsense | 296 | 675 | 8 | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12166297)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11611060 |
| GRCz11 | 8 | 11648765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTA[C/T]AGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTT
Long Flanking Sequence:
CCTGGCCAGACAGTTAAGAGTGGAAAAAGAAAGAGAGGAATCACTCGCTCATCAGAAACAGGAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTA[C/T]AGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGGTGAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14146
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Nonsense | 306 | 675 | 8 | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12166327)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11611090 |
| GRCz11 | 8 | 11648795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGGTGRTGCAGTACCTACARAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTKGAGGACAAGGTGAGCTTTTAAAGGGATAGT
Long Flanking Sequence:
AAGAGAGGAATCACTCGCTCATCAGAAACAGGAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTACAGAAGGTGGCGTCTGAGCCTGCTATGGGC[C/T]AGGCAGAACTGAGGGAGCTTGAGGACAAGGTGAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGTAATATTGTGAAAAAAGCAGACATTCATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34331
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004288 | Essential Splice Site | 315 | 675 | None | 18 |
The following transcripts of ENSDARG00000007444 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12166358)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11611121 |
| GRCz11 | 8 | 11648826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGG[T/C]GAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTC
Long Flanking Sequence:
GAGCAGAAAAACCAGGTAGAGACCAAGAGTTTGCATGTTTGCAGGAAATCGAAGAGTTATTATCTATTTTCAAGTATCAAGTATCTGCTAGGCATTCCGATAACATAGATTGTGTTTCGTCTCTTCTGTAGCTCTTCCAGGCAGAGCAGAGACTGCAGAGATGTCAGATCCAGCTCAAAGACTTACAGCAGGCAGCAGCAGACGAAAAGCCAGAGAGTAAGTTAATTCGCCTAAGGAAACCTTTCCCTGAATGACTCATTACTTTGGTTAATAATAAGATGCCTTCAGTATTTTACTTTTTCGAAAGGTAACATGCATGTGTTCTTAAACCATAGGCCTTATGAAGAGACTTGAGGAGGACATTAAGTTCAACTCCTACATGGTGTCTGAGAAGCTCCCCAGAGAGTTGGAGAATATGAGAAAGGTGGTGCAGTACCTACAGAAGGTGGCGTCTGAGCCTGCTATGGGCCAGGCAGAACTGAGGGAGCTTGAGGACAAGG[T/C]GAGCTTTTAAAGGGATAGTTCCTATTTTACAGGAGATACTCAAACTGTTCAAACTGGTTCTGTTTATACACCTACTCACATATCGTATAATCAACTAAATGAAACAAAGTAAGTATCTAAAGACTTTTTATTATAAGTTTTAGTCAAGAAGACATATTCTGTTAAAGGGATAGTTGACCCGAAAATTGAAAATAGTAGGAAATACTATTGAAGTCAATGCTTACAGGACTCCAGCTTTCTTCAAAGCTTGTTCTTTAGTGTTTAACAGAAGAAAGAAACTCAAAAAAGCTTTGGAACGATATGGGTGAGTAAATTATAACATAATTTTCAGTTTTGGGTGAACGGTCCCTTTAAGACGGAAGTTTGAACTTGAGTACTCTTCCAGTAAAAGTTTAAGATTGGTAGGATTTTTTTACCATGAAAGTTCAGTATAATCAGTAATATTGTGAAAAAAGCAGACATTCATTTTTTTTTTCAGCTTAGTCCGTTTATTAATCTAG
Associated Phenotype:
Not determined